Cell Discovery · 2020 · 192 citations · 42 references
Life SciencesBiologyMolecular BiologyMolecular VirologyStructural BiologyVirologyAnimal VirusesViral AttachmentViral InfectionsViral TropismVirus StructureBinding Mode AnalysisCo-receptor BindingCryo-electron Microscopy ReconstructionIntermediate Host EvolutionIntermediate Host RangeSars-cov-2 InfectionSevere Acute Respiratory SyndromeVirus Receptor-binding Structures
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of the recent pandemic COVID-19, is reported to have originated from bats, with its intermediate host unknown to date. Here, we screened 26 animal counterparts of the human ACE2 (hACE2), the receptor for SARS-CoV-2 and SARS-CoV, and found that the ACE2s from various species, including pets, domestic animals and multiple wild animals, could bind to SARS-CoV-2 receptor binding domain (RBD) and facilitate the transduction of SARS-CoV-2 pseudovirus. Comparing to SARS-CoV-2, SARS-CoV seems to have a slightly wider range in choosing its receptor. We further resolved the cryo-electron microscopy (cryo-EM) structure of the cat ACE2 (cACE2) in complex with the SARS-CoV-2 RBD at a resolution of 3 Å, revealing similar binding mode as hACE2 to the SARS-CoV-2 RBD. These results shed light on pursuing the intermediate host of SARS-CoV-2 and highlight the necessity of monitoring susceptible hosts to prevent further outbreaks.
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